clindamycin hydrochloride
Generic: clindamycin hydrochloride
Labeler: major pharmaceuticalsDrug Facts
Product Profile
Brand Name
clindamycin hydrochloride
Generic Name
clindamycin hydrochloride
Labeler
major pharmaceuticals
Dosage Form
CAPSULE
Routes
Active Ingredients
clindamycin hydrochloride 150 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0904-5959
Product ID
0904-5959_6bac37f8-6c52-432c-8840-0a8b6ef027e7
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA065061
Listing Expiration
2026-12-31
Marketing Start
2009-04-10
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
09045959
Hyphenated Format
0904-5959
Supplemental Identifiers
RxCUI
UNII
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
clindamycin hydrochloride (source: ndc)
Generic Name
clindamycin hydrochloride (source: ndc)
Application Number
ANDA065061 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 150 mg/1
Packaging
- 100 BLISTER PACK in 1 CARTON (0904-5959-61) / 1 CAPSULE in 1 BLISTER PACK
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6bac37f8-6c52-432c-8840-0a8b6ef027e7", "openfda": {"unii": ["T20OQ1YN1W"], "rxcui": ["197518"], "spl_set_id": ["f9e6ed50-ad03-4a9e-8760-8733e04a058c"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-5959-61) / 1 CAPSULE in 1 BLISTER PACK", "package_ndc": "0904-5959-61", "marketing_start_date": "20090410"}], "brand_name": "Clindamycin hydrochloride", "product_id": "0904-5959_6bac37f8-6c52-432c-8840-0a8b6ef027e7", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Sebaceous Gland Activity [PE]", "Lincosamide Antibacterial [EPC]", "Lincosamides [CS]", "Neuromuscular Blockade [PE]"], "product_ndc": "0904-5959", "generic_name": "Clindamycin hydrochloride", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clindamycin hydrochloride", "active_ingredients": [{"name": "CLINDAMYCIN HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA065061", "marketing_category": "ANDA", "marketing_start_date": "20090410", "listing_expiration_date": "20261231"}